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Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies

✍ Scribed by Willemsen, Marjolein H.; de Leeuw, Nicole; de Brouwer, Arjan P.M.; Pfundt, Rolph; Hehir-Kwa, Jayne Y.; Yntema, Helger G.; Nillesen, Willy M.; de Vries, Bert B.A.; van Bokhoven, Hans; Kleefstra, Tjitske


Book ID
120449469
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
197 KB
Volume
55
Category
Article
ISSN
1769-7212

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